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来自麻黄根的二聚体原花青素。

Dimeric proanthocyanidins from the roots of Ephedra sinica.

作者信息

Tao Huaming, Wang Lishu, Cui Zhanchen, Zhao Daqing, Liu Yonghong

机构信息

College of Chemistry, Jilin University, Changchun, P. R. China.

出版信息

Planta Med. 2008 Dec;74(15):1823-5. doi: 10.1055/s-0028-1088321. Epub 2008 Oct 30.

Abstract

Two new dimeric proanthocyanidins, ephedrannin B ( 2) and mahuannin E ( 4), along with two known congeners, ephedrannin A ( 1) and mahuannin D ( 3), were isolated from the roots of Ephedra sinica Stapf. Based on NMR, MS, and CD analysis, the structures of the new compounds were deduced to be 5,7,4'-trihydroxyflavan-[4(alpha)-->8,2(alpha)-->O-->7]-kaempferol ( 2) and 5,7,4'-trihydroxyflavan-[4(beta)-->8,2(beta)-->O-->7]- EPI-afzelechin ( 4). The compounds 1 - 4 were evaluated for cytotoxicity against three tumor cell lines (SGC-7901, HepG2, and HeLa), and 2 was found to be significantly active.

摘要

从麻黄(Ephedra sinica Stapf)的根部分离出两种新的二聚体原花青素,麻黄宁B(2)和麻黄酮E(4),以及两种已知的同系物,麻黄宁A(1)和麻黄酮D(3)。基于核磁共振(NMR)、质谱(MS)和圆二色光谱(CD)分析,推断出新化合物的结构分别为5,7,4'-三羟基黄烷-[4(α)→8,2(α)→O→7]-山奈酚(2)和5,7,4'-三羟基黄烷-[4(β)→8,2(β)→O→7]-表阿夫儿茶素(4)。对化合物1 - 4进行了针对三种肿瘤细胞系(SGC - 7901、HepG2和HeLa)的细胞毒性评估,发现化合物2具有显著活性。

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